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FDA 510(k)

CENTRAL VEINOUS PRESSURE SETS

K-Number: K760386 · 1976-11-02

ApplicantB. Braun Instruments
Decision Date1976-11-02
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL VEINOUS PRESSURE SETS is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun Instruments. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760386. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VEINOUS PRESSURE SETS?

CENTRAL VEINOUS PRESSURE SETS is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is B. Braun Instruments. The 510(k) number is K760386.

When did CENTRAL VEINOUS PRESSURE SETS receive FDA 510(k) clearance?

CENTRAL VEINOUS PRESSURE SETS received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760386.

Who is the listed applicant for CENTRAL VEINOUS PRESSURE SETS?

The FDA 510(k) record lists B. Braun Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRAL VEINOUS PRESSURE SETS?

The FDA product code for CENTRAL VEINOUS PRESSURE SETS is DQO.

Related Clinical Trials

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Other records listing B. Braun Instruments as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K760380INTRAVENOUS TRANSFER SET (INTRAFIX)K760382CONNECTORSK760390CATHETER, VEIN (BRAUNULA T)K760385EXTENSION SETSK760384STOPPERSK760388CATHETER, VEIN (VENOFIX)

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Related Devices (Code: DQO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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